Prevalence of TTR variants detected by whole-exome sequencing in hypertrophic cardiomyopathy. (2019)
Attributed to:
Discovering the causes of mutation-negative hypertrophic cardiomyopathy
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1080/13506129.2019.1665996
PubMed Identifier: 31554435
Publication URI: http://europepmc.org/abstract/MED/31554435
Type: Journal Article/Review
Volume: 26
Parent Publication: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Issue: 4
ISSN: 1350-6129